| Drug NDC: | 64578-0128 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. | |
| Proprietary Name: | Viru-chord |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. | |
| Non Proprietary Name: | Belladonna, Cinchona Officinalis, Echinacea (angustifolia), Gelsemium Sempervirens, Glandula Suprarenalis Suis, Glycyrrhiza Glabra, Hepar Suis, Hydrastis Canadensis, Illicium Anisatum, Influenzinum, Lachesis Mutus, Lappa Major, Magnesia Phosphorica, Morbillinum, Myrrha, Nasturtium Aquaticum, Nux Vomica, Paloondo, Pyridoxinum Hydrochloricum, Riboflavinum, Sambucus Nigra, Scutellaria Lateriflora, Thiaminum Hydrochloricum, Thyroidinum (bovine) |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Energetix Corp |
| Name of Company corresponding to the labeler code segment of the ProductNDC. | |
| Dosage Form: | Liquid |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. | |
| Substance Name: | ARCTIUM LAPPA ROOT - 4 [hp_X]/mL ATROPA BELLADONNA - 12 [hp_X]/mL CINCHONA OFFICINALIS BARK - 12 [hp_X]/mL ECHINACEA ANGUSTIFOLIA - 4 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT - 6 [hp_X]/mL GLYCYRRHIZA GLABRA - 4 [hp_X]/mL GOLDENSEAL - 5 [hp_X]/mL INFLUENZA A VIRUS A/BRISBANE/10/2010 (H1N1) HEMAGGLUTININ ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) - 30 [hp_X]/mL INFLUENZA A VIRUS A/BRISBANE/10/2010 (H1N1) NEURAMINIDASE ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) - 30 [hp_X]/mL INFLUENZA A VIRUS A/SOUTH AUSTRALIA/55/2014 (H3N2) HEMAGGLUTININ ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) - 30 [hp_X]/mL Load more... INFLUENZA A VIRUS A/SOUTH AUSTRALIA/55/2014 (H3N2) NEURAMINIDASE ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) - 30 [hp_X]/mL INFLUENZA B VIRUS B/UTAH/9/2014 HEMAGGLUTININ ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) - 30 [hp_X]/mL INFLUENZA B VIRUS B/UTAH/9/2014 NEURAMINIDASE ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) - 30 [hp_X]/mL LACHESIS MUTA VENOM - 12 [hp_X]/mL LARREA TRIDENTATA LEAF - 12 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE - 12 [hp_X]/mL MEASLES VIRUS - 30 [hp_X]/mL MYRRH - 4 [hp_X]/mL NASTURTIUM OFFICINALE - 6 [hp_X]/mL PORK LIVER - 9 [hp_X]/mL PYRIDOXINE HYDROCHLORIDE - 12 [hp_X]/mL RIBOFLAVIN - 12 [hp_X]/mL SAMBUCUS NIGRA FLOWERING TOP - 4 [hp_X]/mL SCUTELLARIA LATERIFLORA - 6 [hp_X]/mL STAR ANISE - 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED - 12 [hp_X]/mL SUS SCROFA ADRENAL GLAND - 9 [hp_X]/mL THIAMINE HYDROCHLORIDE - 12 [hp_X]/mL THYROID, BOVINE - 9 [hp_X]/mL |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. | |
| Route Details: | ORAL |
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Marketing Start Date: | 01 Jun, 2016 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 25 Dec, 2025 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. | |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. | |
| Manufacturer Name: | Energetix Corp |
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. | |
| Original Packager: | Yes |
| Whether or not the drug has been repackaged for distribution. | |
| NUI: | N0000185371 N0000185375 N0000175629 N0000184306 M0000728 M0006342 M0016962 N0000185001 M0516536 |
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). | |
| UNII: | 597E9BI3Z3 WQZ3G9PF0H S003A158SB VB06AV5US8 639KR60Q1Q 2788Z9758H ZW3Z11D0JV KFL1W6W9JB 80T3QS071U V3EC8AF8MF Load more... 445486QJCG 9VVQ21KI5Z 3W5C8YUT4D VSW71SS07I PK0TXD049P HF539G9L3Q HT3R7C012Q JC71GJ1F3L YH89GMV676 6EC706HI7F 68Y4CF58BV TLM2976OFR CT03BSA18U 7BP4DH5PDC XKC1657P78 269XH13919 398IYQ16YV M572600E5P MN18OTN73W |
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. | |
| Pharmacologic Class EPC: | Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] |
| Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`. | |
| Pharmacologic Class PE: | Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE] |
| Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`. | |
| Pharmacologic Class CS: | Allergens [CS] Dietary Proteins [CS] Plant Proteins [CS] Seed Storage Proteins [CS] |
| Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient]. | |
| Pharmacologic Class: | Allergens [CS] Analogs/Derivatives [Chemical/Ingredient] Calculi Dissolution Agent [EPC] Cell-mediated Immunity [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Increased IgG Production [PE] Increased Large Intestinal Motility [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Inhibition Small Intestine Fluid/Electrolyte Absorption [PE] Magnesium Ion Exchange Activity [MoA] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Osmotic Activity [MoA] Osmotic Laxative [EPC] Plant Proteins [CS] Seed Storage Proteins [CS] Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] Vitamin B 6 [Chemical/Ingredient] Vitamin B6 Analog [EPC] |
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. | |
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|---|---|---|---|
| 64578-0128-1 | 59.1 mL in 1 BOTTLE, DROPPER (64578-0128-1) | 01 Jun, 2016 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. | ||||
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